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Project Coordinator With Clinical Operations Jobs in Missouri

Project Coordinator (Clinical Operations)
By GroupA At California, United States
Creation and management of contracts with institutions and vendors
Budget management and accruals and Interfaces with the Accounting Departments to create
Document management (eg Sharepoint, teams, etc)
3+ years of experience within an operational role in the biotechnology/pharmaceutical industry (e.g., medical affairs, clinical operations, clinical research, CRO)
Analytical skills: ability to analyze, sort and prioritize data, create data extracts and or reports from systems
Experience with the following tools: Microsoft Office Suite (Excel, Word, PowerPoint, etc.), MS Teams, Zoom, Ariba, Icertis. SAP, Cybergrants. Smartsheet
Clinical Operations Coordinator Jobs
By Mindlance At California, United States
•Experience with an ERP software, JDE and CTMS (Clinical Trial Management System) preferred
•Good computer skills including MS Office Suite, Adobe, and ability to operate general office machinery
•Good written and verbal communication skills and interpersonal relationship skills
•Ability to manage confidential information with discretion
18+ Month Assignment (possibility of extension)
•Conduct periodic audits of documentation and may participate in internal master file audits

Are you looking for an exciting opportunity to join a dynamic team and make a real impact? We are looking for a Project Coordinator with Clinical Operations experience to join our team and help us drive our clinical operations forward. You will be responsible for coordinating and managing clinical operations projects, ensuring that all project timelines and deliverables are met. If you have a passion for clinical operations and are looking for a challenging and rewarding role, then this is the perfect opportunity for you!

Overview Project Coordinators with Clinical Operations are responsible for providing administrative and operational support to clinical research projects. They coordinate the activities of the project team, manage timelines, and ensure that the project is completed on time and within budget. Detailed Job Description Project Coordinators with Clinical Operations are responsible for providing administrative and operational support to clinical research projects. They coordinate the activities of the project team, manage timelines, and ensure that the project is completed on time and within budget. They are also responsible for tracking project progress, preparing reports, and communicating with stakeholders. Project Coordinators with Clinical Operations must have excellent organizational and communication skills, as well as the ability to work independently and as part of a team. They must be able to manage multiple tasks and prioritize work to meet deadlines. Job Skills Required
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize work to meet deadlines
• Knowledge of clinical research processes and regulations
• Proficiency in Microsoft Office Suite
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research or project management
• Knowledge of clinical research processes and regulations
• Proficiency in Microsoft Office Suite
Job Knowledge
• Knowledge of clinical research processes and regulations
• Knowledge of project management principles and techniques
• Knowledge of data analysis and reporting
Job Experience
• At least two years of experience in clinical research or project management
• Experience in coordinating and managing clinical research projects
• Experience in preparing reports and presentations
Job Responsibilities
• Coordinate and manage clinical research projects
• Track project progress and prepare reports
• Communicate with stakeholders and ensure project deadlines are met
• Monitor project budget and ensure that project is completed within budget
• Prepare presentations and other materials for project meetings
• Ensure compliance with clinical research regulations and guidelines